JP6162480B2 - 硬化性組成物 - Google Patents
硬化性組成物 Download PDFInfo
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- JP6162480B2 JP6162480B2 JP2013105532A JP2013105532A JP6162480B2 JP 6162480 B2 JP6162480 B2 JP 6162480B2 JP 2013105532 A JP2013105532 A JP 2013105532A JP 2013105532 A JP2013105532 A JP 2013105532A JP 6162480 B2 JP6162480 B2 JP 6162480B2
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical group OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000005004 perfluoroethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 150000004980 phosphorus peroxides Chemical class 0.000 description 1
- 238000007539 photo-oxidation reaction Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
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- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002627 poly(phosphazenes) Polymers 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
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- 229920000379 polypropylene carbonate Polymers 0.000 description 1
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- 239000004814 polyurethane Substances 0.000 description 1
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- 238000004382 potting Methods 0.000 description 1
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- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
- JTQPTNQXCUMDRK-UHFFFAOYSA-N propan-2-olate;titanium(2+) Chemical compound CC(C)O[Ti]OC(C)C JTQPTNQXCUMDRK-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- BPJZKLBPJBMLQG-KWRJMZDGSA-N propanoyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OC(=O)CC BPJZKLBPJBMLQG-KWRJMZDGSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
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- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
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- 229910002027 silica gel Inorganic materials 0.000 description 1
- 125000005371 silicon functional group Chemical group 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical class S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical compound Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- XSIGLRIVXRKQRA-UHFFFAOYSA-N triethoxysilylmethanethiol Chemical compound CCO[Si](CS)(OCC)OCC XSIGLRIVXRKQRA-UHFFFAOYSA-N 0.000 description 1
- QYBKVVRRGQSGDC-UHFFFAOYSA-N triethyl methyl silicate Chemical compound CCO[Si](OC)(OCC)OCC QYBKVVRRGQSGDC-UHFFFAOYSA-N 0.000 description 1
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
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Description
反応性ケイ素基を含有する有機重合体は、室温においても湿分等により反応し、反応性ケイ素基のシロキサン縮合反応によって、分子量増大や架橋を成しえる。その結果、粘着性能を発現したり、ゴム状硬化物が得られることが知られている。
(1).
シロキサン結合を形成することにより架橋し得るケイ素含有基を有する有機重合体(A)、エポキシ樹脂(B)、および、エポキシ樹脂硬化剤(C)を含有する硬化性組成物であって、エポキシ樹脂(B)が有機重合体(A)100重量部に対して5〜40重量部であり、かつエポキシ樹脂硬化剤(C)が有機重合体(A)100重量部に対して5〜30重量部かつエポキシ樹脂(B)100重量部に対して40〜100重量部である硬化性組成物、
(2).
エポキシ樹脂硬化剤(C)が1級アミノ基を構造に持たない(1)に記載の硬化性組成物、
(3).
エポキシ樹脂硬化剤(C)が3級アミンである(1)または(2)のいずれかに記載の硬化性組成物、
(4).
有機重合体(A)の主鎖がオキシアルキレン系重合体、および(メタ)アクリル酸エステル系重合体、飽和炭化水素系重合体からなる群から選択される1種以上である(1)〜(3)のいずれかに記載の硬化性組成物、
(5).
更にシラノール縮合触媒(D)を含有する(1)〜(4)のいずれかに記載の硬化性組成物、
(6).
更にシランカップリング剤(E)を含有する(1)〜(5)のいずれかに記載の硬化性組成物、
(7).
更に可塑剤(F)を含有することを特徴とする(1)〜(6)のいずれかに記載の硬化性組成物、
(8).
硬化性組成物が、前記有機重合体(A)、エポキシ樹脂硬化剤(C)、および、アミノシラン(E)を含有するA剤と、エポキシ樹脂(B)、シラノール縮合触媒(D)、可塑剤(F)、および、水を含有するB剤とからなる2液型である(7)に記載の硬化性組成物、
(9).
前記(1)から(8)のいずれかに記載の硬化性組成物を建築物の下地に直接塗布することを特徴とする防水工法、
(10).
前記(1)から(8)のいずれかに記載の硬化性組成物を硬化させてなる塗膜の上に、トップコートを塗布する防水工法、
に関する。
有機重合体(A)の反応性ケイ素基は、一般式(1):
−SiR1 3−aXa (1)
(R1は、それぞれ独立に炭素原子数1から20の置換あるいは非置換のアルキル基、炭素原子数6から20のアリール基、炭素原子数7から20のアラルキル基、または、−OSiR’3(R’は、それぞれ独立に炭素原子数1から20の炭化水素基である)で示されるトリオルガノシロキシ基である。また、Xは、それぞれ独立にヒドロキシ基または加水分解性基である。更に、aは1から3の整数である)で表される。
反応性ケイ素基含有有機重合体(A)に含有される反応性ケイ素基は、重合体1分子中に平均して、下限は1.2個以上が好ましく、1.3個以上がより好ましく、1.4個以上が特に好ましい。上限は5個以下であることが好ましく、4個以下がより好ましく、3個以下が特に好ましい。(A)成分に含有される反応性ケイ素基が少ないと、硬化したシートの硬度が低くなりすぎ、耐久性が低下する傾向がある。一方、反応性ケイ素基が多いと、硬度が高くなりすぎ、柔軟性や伸縮性が低下する傾向がある。特に低温において脆いシートとなるため適さない傾向にある。
−R2−O− (2)
(R2は、炭素原子数1から14の直鎖状もしくは分岐アルキレン基である)で示される繰り返し単位を有する重合体であり、重合体の全ての繰り返し単位中に一般式(2)で表される繰り返し単位が50重量%以上存在することが好ましい。一般式(2)におけるR2は、炭素原子数1から14の、更には2から4の、直鎖状もしくは分岐アルキレン基が好ましい。一般式(2)で示される繰り返し単位の具体例としては、
−CH2O−、−CH2CH2O−、−CH2CH(CH3)O−、−CH2CH(C2H5)O−、−CH2C(CH3)2O−、−CH2CH2CH2CH2O−
等が挙げられる。ポリオキシアルキレン系重合体の主鎖骨格は、1種類だけの繰り返し単位からなってもよいし、2種類以上の繰り返し単位からなってもよい。特にシーリング材等に使用される場合には、プロピレンオキシド重合体を主成分とする重合体から成るものが非晶質であることや比較的低粘度である点から好ましい。
−CH2−C(R3)(COOR4)− (3)
(R3は水素原子またはメチル基、R4は炭素原子数1から8のアルキル基を示す)で表される炭素原子数1から8のアルキル基を有する(メタ)アクリル酸エステル単量体単位と、下記一般式(4):
−CH2−C(R3)(COOR5)− (4)
(R3は前記に同じ、R5は炭素原子数9以上のアルキル基を示す)で表される炭素原子数9以上のアルキル基を有する(メタ)アクリル酸エステル単量体単位からなる共重合体に、反応性ケイ素基を有するポリオキシアルキレン系重合体をブレンドして製造する方法である。
該共重合体に含有されていてもよい一般式(3)および一般式(4)以外の単量体単位としては、例えば、アクリル酸、メタクリル酸等のアクリル酸;アクリルアミド、メタクリルアミド、N−メチロールアクリルアミド、N−メチロールメタクリルアミド等のアミド基、グリシジルアクリレート、グリシジルメタクリレート等のエポキシ基、ジエチルアミノエチルアクリレート、ジエチルアミノエチルメタクリレート、アミノエチルビニルエーテル等のアミノ基を含む単量体;その他アクリロニトリル、スチレン、α−メチルスチレン、アルキルビニルエーテル、塩化ビニル、酢酸ビニル、プロピオン酸ビニル、エチレン等に起因する単量体単位があげられる。
−NR6−C(=O)− (5)
(R6は炭素数1から20個の有機基または水素原子を表す)で表される基である。この構造は極性が比較的高いため、硬化物の強度や基材への接着性が高くなる傾向にあり望ましい。
W−R7−SiR1 3−aXa (6)
(R1、X、aは前記と同じ。R7は2価の有機基であり、より好ましくは炭素原子数1から20の炭化水素基である。Wはヒドロキシ基、カルボキシ基、メルカプト基およびアミノ基(1級または2級)から選ばれた活性水素含有基である)で表されるケイ素化合物のW基を反応させる方法により製造されるものを挙げることができる。この製造方法に関連した、有機重合体の公知の製造法を例示すると、特公昭46−12154号(米国特許3632557号)、特開昭58−109529号(米国特許4374237号)、特開昭62−13430号(米国特許4645816号)、特開平8−53528号(EP0676403)、特開平10−204144号(EP0831108)、特表2003−508561(米国特許6197912号)、特開平6−211879号(米国特許5364955号)、特開平10−53637号(米国特許5756751号)、特開平11−100427号、特開2000−169544号、特開2000−169545号、特開2002−212415号、特許第3313360号、米国特許4067844号、米国特許3711445号、特開2001−323040号等が挙げられる。
O=C=N−R7−SiR1 3−aXa (7)
(R7、R1、X、aは前記に同じ)で示される反応性ケイ素基含有イソシアネート化合物とを反応させることにより製造されるものを挙げることができる。この製造方法に関連した、有機重合体の公知の製造法を例示すると、特開平11−279249号(米国特許5990257号)、特開2000−119365号(米国特許6046270号)、特開昭58−29818号(米国特許4345053号)、特開平3−47825号(米国特許5068304号)、特開平11−60724号、特開2002−155145号、特開2002−249538号、WO03/018658、WO03/059981等が挙げられる。
本発明では、可塑剤(F)を使用してもよい。可塑剤の例としては、ジオクチルアジペート、ジオクチルセバケート、ジブチルセバケート、コハク酸ジイソデシル等の非芳香族二塩基酸エステル類;オレイン酸ブチル、アセチルリシリノール酸メチル等の脂肪族エステル類;トリクレジルホスフェート、トリブチルホスフェート等のリン酸エステル類;トリメリット酸エステル類;塩素化パラフィン類;アルキルジフェニル、部分水添ターフェニル、等の炭化水素系油;プロセスオイル類;エポキシ化大豆油、エポキシステアリン酸ベンジル等のエポキシ可塑剤類をあげることができる。
鱗片状または粒状の物質としては、ケイ砂、マイカ等の天然物、合成ゴム、合成樹脂、アルミナ等の無機物が使用される。目地部に充填した際の意匠性を高めるために、外壁の材質、模様等に合わせて、適当な色に着色される。
本発明の硬化性組成物には、必要に応じて垂れを防止し、作業性を良くするためにチクソ性付与剤(垂れ防止剤)を添加しても良い。垂れ防止剤としては特に限定されないが、例えば、ポリアミドワックス類;水添ヒマシ油誘導体類;ステアリン酸カルシウム、ステアリン酸アルミニウム、ステアリン酸バリウム等の金属石鹸類等が挙げられる。また、特開平11−349916号公報に記載されているような粒子径10から500μmのゴム粉末や、特開2003−155389号公報に記載されているような有機質繊維を用いると、チクソ性が高く作業性の良好な組成物が得られる。これらチクソ性付与剤(垂れ防止剤)は単独で用いてもよく、2種以上併用してもよい。チクソ性付与剤は(A)成分100重量部に対して、0.1から20重量部の範囲で使用される。
数平均分子量が約2,000のポリプロピレングリコールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてプロピレンオキシドの重合を行い、数平均分子量約14,600(送液システムとして東ソー製HLC−8120GPCを用い、カラムは東ソー製TSK−GEL Hタイプを用い、溶媒はTHFを用いて測定したポリスチレン換算分子量)のポリプロピレンオキシドを得た。続いて、この水酸基を有するポリプロピレンオキシドの水酸基に対して1.2倍当量のNaOMeのメタノール溶液を添加してメタノールを留去し、更にポリプロピレンオキシドの水酸基に対して2.0倍当量の塩化アリルを添加して末端の水酸基をアリル基に変換した。
得られたアリル基を有するポリプロピレンオキシド(P−1)100重量部に対し、白金ビニルシロキサン錯体の白金含量3wt%のイソプロパノール溶液45ppmを触媒として、トリエトキシシラン2.8重量部と90℃で2時間反応させ、1分子あたり平均して1.6個のトリエトキシシリル基を有するポリプロピレンオキシドを得た。
得られたトリエトキシシリル基を有するポリプロピレンオキシド100重量部に対し、0.5wt%の塩酸のメタノール溶液0.24重量%を触媒として使用し、20重量部のメタノールを添加して70℃で2時間混合攪拌して、末端のトリエトキシシリル基をトリメトキシシリル基に変換し、エタノールを減圧脱揮することにより、1分子あたり平均して1.6個のトリメトキシシリル基を有するポリプロピレンオキシド(A−1)を得た。
分子量約2,000のポリオキシプロピレンジオールと分子量約3,000のポリオキシプロピレントリオールの1/1(重量比)混合物を開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてプロピレンオキシドの重合を行い、数平均分子量約19,000のポリプロピレンオキシドを得た。続いて、この水酸基を有するポリプロピレンオキシドの水酸基に対して1.2倍当量のNaOMeのメタノール溶液を添加してメタノールを留去し、更にポリプロピレンオキシドの水酸基に対して2.0倍当量の塩化アリルを添加して末端の水酸基をアリル基に変換した。
合成例1で得られたアリル基末端ポリプロピレンオキシド(P−1)100重量部に対し、白金ビニルシロキサン錯体の白金含量3wt%のイソプロパノール溶液36ppmを触媒として、メチルジメトキシシラン1.8重量部と90℃で2時間反応させ、1分子あたり平均して1.6個のメチルジメトキシシリル基を有するポリプロピレンオキシド(A−3)を得た。
(合成例4)
数平均分子量が約3,000のポリオキシプロピレントリオールを開始剤とし、亜鉛ヘキサシアノコバルテートグライム錯体触媒にてプロピレンオキシドの重合を行い、数平均分子量約26,000のポリプロピレンオキシドを得た。続いて、この水酸基を有するポリプロピレンオキシドの水酸基に対して1.2倍当量のNaOMeのメタノール溶液を添加してメタノールを留去し、更にポリプロピレンオキシドの水酸基に対して2.0倍当量の塩化アリルを添加して末端の水酸基をアリル基に変換した。
表1に示す処方に従って、合成例1〜4で得られた反応性ケイ素基含有有機重合体(A−1〜4)、エポキシ硬化剤、シランカップリング剤、脱水剤をそれぞれ計量し、脱水条件下にて実質的に水分の存在しない状態で混練した後、防湿性の容器に密閉し、2液型組成物のA剤を得た。次に、表1に示す処方に従って、エポキシ樹脂、可塑剤、充填剤、酸化防止剤、シラノール縮合触媒、水、分散剤をそれぞれ計量し、ミキサーを用いて、よく混練した後、容器に密閉し、2液型組成物のB剤を得た。表1の2液型組成物は、使用時にA剤とB剤の各容器から所定量取り出し、後述の評価を行った。
<エポキシ硬化剤>アンカミンK−54(エアープロダクツ社製、2,4,6−トリス(ジメチルアミノメチル)フェノール)
<シランカップリング剤>Dynasylan AMMO(EVONIK社製、γ−アミノプロピルトリメトキシシラン)
<脱水剤>Dynasylan VTMO(EVONIK社製、ビニルトリメトキシシラン)
<エポキシ樹脂>jER828(三菱化学社製、ビスフェノールA型エポキシ樹脂)
<可塑剤>アクトコール21−56(三井化学社製、分子量2000のジオール型ポリプロピレングリコール)
<充填剤>Carbital110S(IMERYS社製、ステアリン酸処理重質炭酸カルシウム)Lampblack101(Evonik社製、カーボンブラック)
<酸化防止剤>イルガノックス245(チバ・スペシャルティ・ケミカルズ社製)
<シラノール縮合触媒>TIB KAT216(TIB Chemicals社製、ジオクチル錫ジラウレート)
<分散剤>DA−375(楠本化成社製、ポリエーテル燐酸エステル)。
上記硬化性組成物を厚さ3mmのシート状型枠に充填し23℃、50%RH条件で7日間静置しシート状硬化物を作成した。また、23℃、50%RH7日の後、さらに50℃乾燥機で7日間養生した硬化物も作成した。23℃7日後と50℃7日後のシートから、JIS K 6251に準拠して3号ダンベル型に打ち抜いた後、島津(株)製オートグラフを用いて引張速度500mm/分で引張試験を行い、100%モジュラス、破断時の伸び(それぞれ、M100、EBと示す)を測定した。得られたM100とEBの値を用いて23℃7日後とさらに50℃7日養生後の変化率を次式から算出した。
(23℃7日後の値)/(50℃7日後の値)×100=変化率(%)。
上記の引張物性と同様の作製方法で得たシート状試験体を23℃、50%RH条件で7日間養生することにより硬化物を得た。得られた硬化物から、JIS K 6251に準拠してアングル形に打ち抜いた後、島津(株)製オートグラフを用いて引張速度500mm/分で引裂き試験を行い、引裂き強度を測定した。
上記硬化性組成物をモルタルに、23℃50%RH条件下にて、およそ縦30mm×横15mm×厚み10mmになるように密着させ、同条件下に7日間置いた後、90度ハンドピール試験により接着性を評価した。凝集破壊を○、界面破壊を×とした。
Claims (10)
- シロキサン結合を形成することにより架橋し得るケイ素含有基を有する有機重合体(A)、エポキシ樹脂(B)、および、エポキシ樹脂硬化剤(C)を含有する硬化性組成物であって、エポキシ樹脂(B)が有機重合体(A)100重量部に対して5〜40重量部であり、かつエポキシ樹脂硬化剤(C)が有機重合体(A)100重量部に対して5〜30重量部かつエポキシ樹脂(B)100重量部に対して40〜100重量部であり、
前記エポキシ樹脂硬化剤(C)が3級アミンであり、
建築物の下地に防水層を形成させる防水工法において、硬化により前記防水層を形成するために用いられる硬化性組成物。 - エポキシ樹脂硬化剤(C)が1級アミノ基を構造に持たない請求項1に記載の硬化性組成物。
- 有機重合体(A)の主鎖がオキシアルキレン系重合体、および(メタ)アクリル酸エステル系重合体、飽和炭化水素系重合体からなる群から選択される1種以上である請求項1または2に記載の硬化性組成物。
- 更にシラノール縮合触媒(D)を含有する請求項1〜3のいずれかに記載の硬化性組成物。
- 更にシランカップリング剤(E)を含有する請求項1〜4のいずれかに記載の硬化性組成物。
- 更に可塑剤(F)を含有することを特徴とする請求項1〜5のいずれかに記載の硬化性組成物。
- 硬化性組成物が、前記有機重合体(A)、エポキシ樹脂硬化剤(C)、および、アミノシラン(E)を含有するA剤と、エポキシ樹脂(B)、シラノール縮合触媒(D)、可塑剤(F)、および、水を含有するB剤とからなる2液型である請求項6に記載の硬化性組成物。
- カオリン、クレー、タルク、マイカの1種または2種以上を含まない、請求項1〜7のいずれか1項に記載の硬化性組成物。
- シロキサン結合を形成することにより架橋し得るケイ素含有基を有する有機重合体(A)、エポキシ樹脂(B)、および、エポキシ樹脂硬化剤(C)を含有する硬化性組成物であって、エポキシ樹脂(B)が有機重合体(A)100重量部に対して5〜40重量部であり、かつエポキシ樹脂硬化剤(C)が有機重合体(A)100重量部に対して5〜30重量部かつエポキシ樹脂(B)100重量部に対して40〜100重量部である硬化性組成物を建築物の下地に直接塗布することを特徴とする防水工法。
- 前記請求項1〜8のいずれかに記載の硬化性組成物を硬化させてなる塗膜の上に、トップコートを塗布する防水工法。
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